Primary Site >> Stomach Cancer

Gene >> CSHL1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000309894
Start 63909866:63909866(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.514C>G
AA Mutation p.Gln172Glu(p.Q172E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000309894
Start 63909755:63909755(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778533335
CDS Mutation c.625C>T
AA Mutation p.Arg209Cys(p.R209C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000309894
Start 63910299:63910299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.334C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000309894
Start 63910827:63910827(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.108delT
AA Mutation p.Phe36LeufsTer23(p.F36Lfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000309894
Start 63909909:63909909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.472-1G>T
Mutation Classification Splice_Site
Feature Type Transcript